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Showing results (211-220 of 216) with videos related to

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Journal of Human Genetics|July 25, 2019
Comprehensive genetic analysis of 57 families with clinically suspected Cornelia de Lange syndromeHiromi Aoi, Takeshi Mizuguchi, José Ricard Ceroni, et al.
Hormone Research in Paediatrics|May 28, 2019
Impact of Growth Hormone Therapy on Adult Height in Patients with PTPN11 Mutations Related to Noonan SyndromeAlexsandra C Malaquias, Renata M Noronha, Thaiana T O Souza, et al.
Scientific Reports|September 8, 2018
A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual DisabilityJ R M Ceroni, R L Dutra, R S Honjo, et al.
American Journal of Human Genetics|October 1, 2019
Autosomal-Recessive Mutations in MESD Cause Osteogenesis ImperfectaShahida Moosa, Guilherme L Yamamoto, Lutz Garbes, et al.
Ambio|February 15, 2002
A new vision of ocean biogeochemistry after a decade of the Joint Global Ocean Flux Study (JGOFS)R Anderson, D Archer, U Bathmann, et al.
Human Mutation|November 1, 2020
Efficient detection of copy-number variations using exome data: Batch- and sex-based analysesYuri Uchiyama, Daisuke Yamaguchi, Kazuhiro Iwama, et al.
Pageof 22

Showing results (211-220 of 216) with videos related to

Sort By:
Pageof 22
You have reached the last page of results.This site can display upto 216 results.
Journal of Human Genetics|July 25, 2019
Comprehensive genetic analysis of 57 families with clinically suspected Cornelia de Lange syndromeHiromi Aoi, Takeshi Mizuguchi, José Ricard Ceroni, et al.
Hormone Research in Paediatrics|May 28, 2019
Impact of Growth Hormone Therapy on Adult Height in Patients with PTPN11 Mutations Related to Noonan SyndromeAlexsandra C Malaquias, Renata M Noronha, Thaiana T O Souza, et al.
Scientific Reports|September 8, 2018
A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual DisabilityJ R M Ceroni, R L Dutra, R S Honjo, et al.
American Journal of Human Genetics|October 1, 2019
Autosomal-Recessive Mutations in MESD Cause Osteogenesis ImperfectaShahida Moosa, Guilherme L Yamamoto, Lutz Garbes, et al.
Ambio|February 15, 2002
A new vision of ocean biogeochemistry after a decade of the Joint Global Ocean Flux Study (JGOFS)R Anderson, D Archer, U Bathmann, et al.
Human Mutation|November 1, 2020
Efficient detection of copy-number variations using exome data: Batch- and sex-based analysesYuri Uchiyama, Daisuke Yamaguchi, Kazuhiro Iwama, et al.
Pageof 22